Global Regulatory Toxicologist

Vor 4 Tagen

Munich, Deutschland Corteva Vollzeit

**Description**:
At Corteva Agriscience, we grow what matters by putting consumers and customers at the heart of everything we do. We recognize that safe and sustainable food is a priority of our consumers, and we're here to ensure those goals are met. As a Global Regulatory Toxicologist at Corteva, you will be an integral part of a growing, multidisciplinary team that is responsible for development, registration, and re-registration of new and existing crop protection products, covering conventional and biological solutions, seeds and integrated agricultural solutions.

How will you help us grow? It matters to us, and it matters to you.

As a member of our Corteva Regulatory Toxicology team, you will operate as a Global Regulatory Toxicology Subject Matter Expert (SME) to:
**Global Regulatory Toxicologist Role and Responsibilities**
- Work collaboratively and across teams (regulatory toxicology, mammalian toxicology, predictive safety) to lead the development of scientific strategies and deliver global toxicology programs.
- Responsible for the design and interpretation of toxicology studies for Corteva active substances and end-use products in support of global regulatory submissions while ensuring the highest standards of scientific practice and animal welfare are met.
- Provide expertise and support for incorporation of robust study summaries and expert positions into the toxicology portion of the registration dossier and author technical responses and Weight of Evidence assessments to regulatory agencies.
- Act as a regulatory toxicology liaison with registration colleagues and technical experts across a wide range of disciplines within the company and national or international regulatory authorities.
- Participate and represent Corteva as a technical expert on industry associations and working groups.
- Additional opportunities for scientific growth within this collaborative, team-based role, include mentoring early career scientists, leading on cross-active ingredient projects, program management, innovative/alternative & mechanistic toxicity testing approaches. and communicating data to a wide variety of audiences.

LI-OB1 #LI-Remote

**Qualifications**:** Requirements**
- A technical background and practical experience(s) in the following areas: general toxicology, endocrine biology, systems biology, new approach methodologies, and/or developmental and reproductive toxicology, is highly desirable for this position.

**The following skills are integral to the successful fulfillment of this position**:

- Application of project leadership skills to collaborate and coordinate multiple projects in a timely and effective manner.
- Effective inter-personal skills and demonstrated teamwork abilities are key to this global role, to create and maintain collaborative and inclusive relationships, positively influence decision-making processes, while keeping teams engaged and motivated to deliver and develop.
- Clear written and oral communication skills that allow dissemination of complex technical issues in a straightforward and concise manner, along with the ability to adapt this information to a variety of scientific and non-scientific audiences both internally and externally.

  • Senior Regulatory Toxicologist

    vor 1 Woche

    Munich, Bayern, Deutschland Corteva Vollzeit

    Description: Senior Regulatory ToxicologistThis position is ideally based in our European Development Centre, near to Oxford (UK) or Munich (DE), but other locations in Europe may be consideredAt Corteva Agriscience, we grow what matters by putting consumers and customers at the heart of everything we do. We recognize that safe and sustainable food is a...

  • Global Regulatory Ecotoxicologist

    vor 3 Wochen

    Munich, Deutschland Corteva Vollzeit

    **Description**: We're hiring a **Global Regulatory Ecotoxicologist**. Learn how you can be our voice in the conversation about the future of agriculture. You will represent the Ecotoxicology Team on multidisciplinary regulatory teams responsible for development, registration or re-registration of new and existing crop protection products. **You Will Be...

  • Manager Global Regulatory Affairs

    vor 1 Woche

    Munich, Deutschland Leaman Life Sciences Vollzeit

    An exciting opportunity to join a well-known regulatory consultancy in Europe that boasts the opportunity to support several regulatory activities for Pharmaceutical and Biotech Clients globallyThe Regulatory Project Manager will play a pivotal role in ensuring that regulatory activities from early development through to dossier preparation for MMA and/or...

  • Associate Regulatory Affairs

    vor 2 Monaten

    Munich, Deutschland Daiichi-Sankyo Europe Vollzeit

    **Passion for Innovation. Compassion for Patients.**: ***Associate Regulatory Affairs - EU Regulatory Procedural Management (M/F/x)***: - limited until 31.10.2024 -**: **The position**: Provide support for EU Regulatory Procedural Management for assigned projects including all pre - and post-authorisation activities ensuring a smooth run of regulatory...

  • Regulatory Affairs Cmc

    Vor 5 Tagen

    Munich, Deutschland Stirling Q&R Ltd Vollzeit

    **Position: Regulatory Affairs CMC** **About the Company**: A renowned pharmaceutical consulting firm is currently seeking a Regulatory Affairs CMC expert with a strong background in **small molecules** and pharmaceuticals. This role offers the opportunity to provide expert guidance on regulatory strategies for drug development projects, ensuring adherence...

  • Clinical Regulatory Director

    Vor 2 Tagen

    Munich, Deutschland Leaman Life Sciences Vollzeit

    Clinical Regulatory Director*Based in Munich, Germany*This role supports cross-functional development teams engaged in innovative drug development (including small molecules, biologicals, and ATMPs) at all stages - from research through clinical development to MAA, NDA/BLA submission.ResponsibilitiesProvide strategic regulatory guidance to project...

  • Director Regulatory Affairs Oncology

    vor 2 Monaten

    Munich, Deutschland Daiichi Sankyo Europe Vollzeit

    To provide European regulatory strategy support for assigned projects, products and non-project work. Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of a multi-disciplinary global product team, providing expertise on regulatory matters....

  • Regulatory Reporting, Avp

    Vor 6 Tagen

    Munich, Deutschland State Street Vollzeit

    Who we are looking for: You will be joining the Regulatory Reporting team in the Munich Office, where the Regulatory Reporting is being overseen for EMEA. Regulatory Reporting makes sure that SSBI Intl. GmbH sends reports to local and global supervisors in time and quality. Join us if making your mark in the financial services industry from day one is a...

  • Senior Regulatory Affairs Specialist

    vor 2 Wochen

    Munich, Deutschland Thermo Fisher Scientific Vollzeit

    At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

  • Regulatory Procedural Management and Clinical Trial

    vor 3 Wochen

    Munich, Deutschland Daiichi Sankyo Europe Vollzeit

    With emphasis on product development and regulatory life cycle management in Europe and AMELA (Australia, Middle East, Eastern Europe, Latin America, Africa) this Senior Director position will provide regulatory leadership, guidance, project management and procedural focused strategy and support to assigned projects in a manner that is scientifically sound,...

  • Director Regulatory Affairs Companion Diagnostics

    Vor 6 Tagen

    Munich, Deutschland Daiichi Sankyo Europe Vollzeit

    Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic tests and other devices to enhance the value of our oncology pharmaceutical products. The job holder provides innovative approaches to resolve complex regulatory issues and increase speed to patients. **Roles & Responsibilities**: - CDx development:...

  • Regulatory Reporting, Avp

    Vor 5 Tagen

    Munich, Deutschland State Street Corporation Vollzeit

    Regulatory Reporting, AVP **Who we are looking for**: You will be joining the Regulatory Reporting team in the Munich Office, where the Regulatory Reporting is being overseen for EMEA. Regulatory Reporting makes sure that SSBI Intl. GmbH sends reports to local and global supervisors in time and quality. Join us if making your mark in the financial services...

  • Regulatory Procedural Management and Clinical Trial Lead

    vor 2 Monaten

    Munich, Deutschland Daiichi Sankyo Europe Vollzeit

    Passion for Innovation. Compassion for Patients. With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world. In Europe, we focus on two areas: The goal of our Specialty Business...

  • Regulatory Procedural Management and Clinical Trial Lead

    vor 4 Wochen

    Munich, Deutschland Daiichi Sankyo Europe Vollzeit

    Passion for Innovation. Compassion for Patients. With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world. In Europe, we focus on two areas: The goal of our Specialty Business...

  • Regulatory Submissions Technical Advisor

    vor 3 Wochen

    Munich, Deutschland Medpace, Inc. Vollzeit

    Job Summary: Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory Submissions Technical Advisors to join our Site Activation and Maintenance team, within Clinical Operations. This position plays a key role at Medpace, preparing and reviewing regulatory documents and providing strategic regulatory advice...

  • Regulatory Submissions Technical Advisor

    vor 1 Woche

    Munich, Bayern, Deutschland Medpace, Inc. Vollzeit

    Job Summary: Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory Submissions Technical Advisors to join our Site Activation and Maintenance team, within Clinical Operations.This position plays a key role at Medpace, preparing and reviewing regulatory documents and providing strategic regulatory advice to...

  • Regulatory Affairs Manager

    Vor 3 Tagen

    Munich, Bayern, Deutschland Cpl Vollzeit

    Regulatory Affairs Manager - Rest of World Markets - Based in Germany/Ireland/RemoteRole can be relocated in Germany, Ireland or Remote working can be facilitatedThis position will be responsible for ensuring efficient and productive regulatory submissions, as well as assisting and collaborating in strategic drug development program implementation for Rest...

  • Country Regulatory Team Leader

    vor 3 Wochen

    Munich, Deutschland Corteva Vollzeit

    **Description**: Corteva Agriscience, the world's first dedicated agriculture start-up, serves to enrich the lives of those who produce and those who consume, ensuring progress for generations to come. Our employees fulfill this purpose everyday by building/participating in an inclusive culture where we encourage each other to stay curious, think...

  • Director of Regulatory Affairs

    vor 3 Wochen

    Munich, Deutschland Cpl Life Sciences Vollzeit

    **Reference Number**: JO-2304-514347 Director of Regulatory Affairs - (EU Relocation) **Rate**: Negotiable **Job Type**: Permanent **Location**: Munich Director, Regulatory Affairs - Infectious Diseases Munich, Germany /Europe - Relocation Package Provided. **Salary**: Attractive salary plus benefits package (stock options, car allowance, bonus...

  • Regulatory Submissions Specialist, Study Start Up

    vor 4 Wochen

    Munich, Deutschland Meet Recruitment Vollzeit

    50000 EUR - 50000 EUR - Hybrid - Munich, Germany, Germany - Permanent **Exciting Opportunity - Join a Global CRO as a Study Start Up Regulatory Submissions Expert!** We are thrilled to announce a fantastic opportunity to join our mid-size global CRO client as a Study Start Up Regulatory Submissions Specialist based in Munich, Germany. This role is a...